U.S. patent number 8,603,662 [Application Number 13/528,055] was granted by the patent office on 2013-12-10 for deposited microarchitectured battery and manufacturing method.
This patent grant is currently assigned to The Regents of the University of Michigan. The grantee listed for this patent is Fabio Albano, Ann Marie Sastry. Invention is credited to Fabio Albano, Ann Marie Sastry.
United States Patent |
8,603,662 |
Sastry , et al. |
December 10, 2013 |
Deposited microarchitectured battery and manufacturing method
Abstract
A battery includes a first portion including a substrate having
formed thereon a current collector and an anode electrode material.
A second portion is formed on a substrate and includes a current
collector and a cathode electrode material. The first portion is
joined to the second portion and a separator is disposed between
the first portion and the second portion as joined to separate the
anode electrode material from the cathode electrode material. An
electrolyte is placed in contact with the anode electrode material,
the cathode electrode material and the separator.
Inventors: |
Sastry; Ann Marie (Ann Arbor,
MI), Albano; Fabio (Ann Arbor, MI) |
Applicant: |
Name |
City |
State |
Country |
Type |
Sastry; Ann Marie
Albano; Fabio |
Ann Arbor
Ann Arbor |
MI
MI |
US
US |
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Assignee: |
The Regents of the University of
Michigan (Ann Arbor, MI)
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Family
ID: |
39808887 |
Appl.
No.: |
13/528,055 |
Filed: |
June 20, 2012 |
Prior Publication Data
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Document
Identifier |
Publication Date |
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US 20130017433 A1 |
Jan 17, 2013 |
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Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
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12059366 |
Mar 31, 2008 |
8231998 |
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60909183 |
Mar 30, 2007 |
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60938232 |
May 16, 2007 |
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Current U.S.
Class: |
429/129; 429/149;
216/13 |
Current CPC
Class: |
H01M
10/0436 (20130101); H01M 10/052 (20130101); H01M
4/13 (20130101); H01M 6/40 (20130101); H01M
50/209 (20210101); Y02P 70/50 (20151101); Y02E
60/10 (20130101); H01M 10/0525 (20130101) |
Current International
Class: |
H01M
2/14 (20060101); H01M 6/42 (20060101) |
Field of
Search: |
;429/129,149 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
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10346310 |
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Apr 2005 |
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DE |
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2003-503822 |
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Jan 2003 |
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JP |
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2007-513464 |
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May 2007 |
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JP |
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Other References
Office Action from the Japan Patent Office, for Japanese Patent
Application No. 2010-501282, filed on Aug. 7, 2012. cited by
applicant .
Search Report and Written Opinion from the European Patent Office
dated Nov. 13, 2012, for EPO application No. EP 08-74-4796. cited
by applicant.
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Primary Examiner: Apicella; Karie O'Neill
Attorney, Agent or Firm: Ogawa; Richard T. Ogawa P.C.
Government Interests
GOVERNMENT FUNDING
This invention was made with government support under EEC9986866
awarded by the National Science Foundation. The government has
certain rights in the invention.
Parent Case Text
CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a divisional of U.S. application Ser. No.
12/059,366, filed Mar. 31, 2008 now U.S. Pat. No. 8,231,998, which
claims priority to and benefit from U.S. Provisional Patent
Application Ser. Nos. 60/909,183, filed Mar. 30, 2007 entitled
Micromachined Battery and 60/938,232, filed May 16, 2007 entitled
Micromachined Battery, the disclosures of which are hereby
incorporated herein by reference for all purposes.
Claims
We claim:
1. A battery comprising: a first portion of a first substrate over
which a first current collector and an anode electrode are formed;
a second portion of a second substrate over which a second current
collector and a cathode electrode are formed, the second substrate
being different from the first substrate; and a separator placed
between the first portion and the second portion to separate the
anode electrode from the cathode electrode, wherein the first and
second portions are joined by bonding the first and second
substrates to face each other with respect to the separator,
wherein the first substrate is a unitary body and a first cavity is
formed in the unitary body of the first substrate, and the second
substrate is a unitary body and a second cavity is formed in the
unitary body of the second substrate, and wherein the first current
collector and the anode electrode are disposed in the first cavity,
and the second current collector and the cathode electrode are
disposed in the second cavity.
2. The battery of claim 1, wherein each of the anode electrode and
the cathode electrode comprises a highly porous microstructure.
3. The battery of claim 1, further comprising an electrolyte in
contact with the anode electrode, the cathode electrode, and the
separator.
4. The battery of claim 1, wherein each of the first and second
substrates comprises glass.
5. The battery of claim 4, wherein the glass comprises silicon
oxide.
6. The battery of claim 1, wherein the anode electrode comprises a
material selected from zinc, lithium metal (Li), graphite (C), meso
carbon micro beads (MCMB), other carbon intercalation compounds,
and a combination thereof.
7. The battery of claim 1, wherein the cathode electrode comprises
a material selected from silver oxide, lithium manganese oxide
(LiMn.sub.2O.sub.4), lithium iron phosphate (LiFePO.sub.4),
LiNi.sub.xCo.sub.yAl.sub.zO.sub.2,
LiNi.sub.xCo.sub.yMn.sub.zO.sub.2, and a combination thereof.
8. The battery of claim 3, wherein the electrolyte comprises a
material selected from potassium hydroxide (KOH), diethyl carbonate
(DEC), dimethyl carbonate (DMC), ethylene carbonate (EC), ethyl
methyl carbonate (EMC), propylene carbonate (PC), any other
electrolyte that conducts ions and is electrically neutral, and a
combination thereof.
9. A microarchitectured battery comprising: a first
microarchitectured cell coupled to one or more additional
microarchitectured cells, wherein each of the first and additional
microarchitectured cells comprises: a first portion of a first
substrate over which a first thin-film current collector and a
thin-film anode electrode are formed; a second portion of a second
substrate over which a second thin-film current collector and a
thin-film cathode electrode are formed, the second substrate being
different from the first substrate; and a separator placed between
the first portion and the second portion to separate the anode
electrode from the cathode electrode, wherein the first and second
portions are joined by bonding the first and second substrates to
face each other with respect to the separator, wherein the first
substrate is a unitary body and a first cavity is formed in the
unitary body of the first substrate, and the second substrate is a
unitary body and a second cavity is formed in the unitary body of
the second substrate, and wherein the first thin-film current
collector and the thin-film anode electrode are disposed in the
first cavity, and the second thin-film current collector and the
thin-film cathode electrode are disposed in the second cavity.
10. The battery of claim 1, wherein the anode and cathode
electrodes are provided by depositing anode and cathode materials,
respectively, through the use of chemical vapor deposition, plasma
vapor deposition, chemical fluid deposition, electroplating,
sintering, or sputtering.
11. The battery of claim 1, wherein a portion of each of the first
and second substrates is etched or ablated to provide the first or
second cavity in which the first or second current collector and
the anode or cathode electrode are disposed.
12. The battery of claim 11, wherein the first or second cavity is
provided by etching the portion of each of the first and second
substrates with or without masking, or by ablating the portion via
application of a laser.
13. The battery of claim 11, wherein the first or second substrate
includes an upper surface and a lower surface, the first or second
cavity being formed by etching the first or second substrate from
the upper surface toward the lower surface.
14. The battery of claim 3, further comprising a channel disposed
in one or both of the first and second portions, the electrolyte
being provided through the channel.
15. The battery of claim 14, wherein the channel is provided by
micromachine drilling or chemical drilling.
16. The battery of claim 9, wherein each of the thin-film anode
electrode and the thin-film cathode electrode comprises a highly
porous microstructure.
17. The battery of claim 9, further comprising an electrolyte in
contact with the thin-film anode electrode, the thin-film cathode
electrode, and the separator.
18. The battery of claim 17, further comprising a channel disposed
in one or both of the first and second portions, the electrolyte
being provided through the channel.
19. The battery of claim 9, wherein a portion of each of the first
and second substrates is etched or ablated to provide the first or
second cavity in which the first or second thin-film current
collector and the thin-film anode or cathode electrode are
disposed.
Description
TECHNICAL FIELD
This patent relates to energy storage systems. More particularly,
this patent relates to a deposited microarchitectured battery
system and a design and manufacturing method for the same.
BACKGROUND
Many micro-electromechanical systems (MEMS) require a power source
of electrical energy. In some instances electrical power is
provided by a coupled battery or battery system. The size advantage
of the MEMS device is lost if the battery is large. Physical
limitations of the electrode materials, separators, and electrolyte
dictate their separate manufacture, and subsequent coupling of the
battery to the MEMS device.
MEMS technology also has enabled development of fully implantable
medical devices. The power supplies for these devices, however, can
account for up to 85% of the mass and 35% of the volume of these
systems. The smallest commercially available batteries are in the
millimeter (mm) range and utilize zinc or lithium chemistries.
Stainless steel casing is typically used to contain the fluid
electrolyte and the gaseous reaction byproducts.
Further miniaturization of implantable systems requires new battery
technologies with enhanced compatibility with MEMS fabrication
techniques and with MEMS-processing compatible materials and
substrates. Power source selection will also rely on more than the
electrochemistry. Form factor, performance, lifetime, toxicity of
the chemistry and the rate of heat generation must be considered in
the design process. This is particularly true with implantable
systems.
SUMMARY OF THE INVENTION
Embodiments of the present invention relate to microarchitectured
batteries. These batteries can be used to create microscopic
footprints, typically on the order of Imm2, and can be integrated
directly into MEMS devices at the time of manufacture.
Microarchitectured batteries have the potential to overcome the
energy and power limitations of the past for MEMS, and will enable
the widespread utilization of MEMS devices for creating wireless
sensor networks for environmental or bio-medical applications; this
is because power sources can be created which are of the same scale
as other components of the system. By using improved fabrication
processes to deposit battery materials, energy losses can be
reduced and storage capability increased, enabling microbatteries
with sizes that can be integrated with MEMS and meet their lifetime
requirements.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a schematic illustration of a micro-electromechanical
embodiment of the invention.
FIG. 2 section view of a micromachined battery in accordance with
an embodiment of the invention.
FIG. 3 is a schematic illustration of a multiple cell micromachined
battery.
DETAILED DESCRIPTION
MEMS devices may benefit from a thin-film, microarchitectured,
deposited battery that can be manufactured with or in a manner
compatible with the manufacture of the MEMS device. A microbattery
may be manufactured using processing techniques used for MEMS
devices themselves. In this manner, the microbattery may be
manufactured to have a footprint no larger than the device itself,
may be manufactured during the processing or using the same
processing techniques as the MEMS device. The microbattery may be
directly coupled to the MEMS device, eliminating additional process
steps. Other microarchitecturing processes can be applied to the
substrates to create spacing, connections or microchannels for
electrolyte, e.g. laser machining, micro-drilling, micro-cutting or
similar processes. While several embodiments of the invention are
described in connection with battery structures suitable for
combination with MEMS devices, the techniques are scalable to
larger dimensions. Therefore, the present invention can be applied
to the design and manufacture of batteries for integration into
much larger format applications, including larger portable devices
such as cell phones, personal digital assistants (PDAs) and laptop
computers, flat photovoltaic arrays, and large format, high power
prismatic or wound cells which power a large variety of devices,
including vehicles, or to provide load-leveling for grid power
installations.
FIG. 1 illustrates a MEMS device 10 and a coupled micromachined
battery 12. The MEMS device may include a glass, silicon-based
substrate 14, e.g., silicon dioxide (SiO.sub.2); a transducer 16
formed on the substrate 14 and circuitry 18, e.g., a processor,
formed in the substrate 14. A cover 20 may enclose the circuit 18
leaving the transducer exposed. The instant invention is not
limited to the particular structure of the MEMS device or its
intended function, including whether the MEMS device is or includes
a transducer or whether or not the MEMS device includes processing
circuitry or similar structures. Thus, the MEMS device may be
virtually any type of MEMS device that has an electrical power
requirement.
The micromachined battery 12 is coupled to the MEMS device 10, and
the micromachined battery 12 may be bonded, for example, to the
MEMS device 10 using polymer adhesive 19, e.g. two parts epoxy
resin.
FIG. 2 illustrates a microbattery, for example the
microarchitectured battery 12, in section. In this realization, the
substrate has been machined using microdiamond drills to create a
spacing between electrodes suitable to contain solid, gel or liquid
electrolyte. The microarchitectured battery 12 includes a first
section 22 and a second section 24 with a separator 26 positioned
between the two sections. The two sections respectively define an
anode and a cathode and therefore differ at least in the electrode
material. The sections may be secured together by adhesive, for
example a fast curing epoxy resin, with the separator 26 being
disposed in between. The separator 26 may be a membrane formed from
polymer such as Celgard.RTM., or other polymeric membranes with
nanometer sized pores, and may be approximately 25 micrometer
(.mu.m) thick, down to 100 nm.
Electrolyte may be introduced using microfluidic channels 28
(depicted in phantom as these channels are sealed following
introduction of the electrolyte) formed in one or both of the
sections. In a preferred implementation, introduction of the
electrolyte is delayed until the MEMS device is placed into
operation to increase the shelf life and then the usable life of
the device.
Each section 22 and 24 may be formed by the deposition of electrode
material 30 onto a substrate 32. A suitable current collector
structure 34 is also deposited onto the substrate 32 advantageously
during the electrode deposition process or as a follow-on process.
The current collector 34 may be formed to include conductive taps
36 to allow an output of the battery to be coupled to the MEMS
device 10. Deposition of electrode active material may be
accomplished by laser machining, e.g. Nd--YAG laser, or other type
of laser) in combination with pulsed laser deposition (PLD),
electron beam deposition (EBD), chemical vapor deposition (CYD),
physical vapor deposition (PYD), chemical fluid deposition (CFD) or
electroplating, or any combination of the above.
In one realization, and not to limit the general nature of the
microarchitectured battery 12, substrates 32 for the anode and the
cathode, may be prepared by first forming masks using
computer-aided design and printing techniques. A photoresist may be
spin coated onto blank substrate stock, such as wafer stock, and
cured using ultraviolet (UY) light exposure or other method. The
photoresist may be selectively removed by a solvent. The substrate
is then etched to the desired depth using an etchant, such as
fluoridic acid (HF), or other etchant which can uniformly and
controllably remove material
As an alternative to wet etching, laser ablation may be used to
etch the substrate. Laser ablation offers potentially fewer
processing steps and faster processing speeds. However, wet etching
may potentially provide better control of the etched depth, and
depth of the cavity geometry.
The first section 22, in this example, a zinc (Zn) anode, may by
formed using three metal deposition steps. A layer of nickel (Ni)
(not depicted), or other metallic or metal oxide materials, for
adhesion purposes, may be deposited onto the etched substrate
followed by a gold (Au) or other conductive current collector,
e.g., current collector 34. A layer of zinc is then deposited for
the active material, e.g., electrode material 30. In this
embodiment, zinc (Zn), is deposited via aerosol spray deposition of
Zn nanoparticles suspended in petroleum or other distillate. In
accordance with another embodiment, the electrode material 30 may
include a material selected from the group including zinc, lithium
metal (Li), graphite (C), meso carbon micro beads (MCMB), other
carbon intercalation compounds, and a combination thereof.
The second section 24, in this example a silver oxide (AgO)
cathode, may be formed using three metal deposition steps. A layer
of nickel (Ni) (not depicted), or other metallic or metal oxide
material for adhesion purposes, is deposited onto the etched
substrate followed by a gold (Au) or other conductive current
collector, e.g., current collector 34. A layer of silver is then
deposited for the active material, e.g., electrode material 30.
Following placement of the silver active material, the silver is
oxidized to silver oxide. The oxidation may be accomplished by
immersing the structure in hydrogen peroxide (H.sub.2O.sub.2) until
the silver material is sufficiently oxidized. Alternatively,
oxidation of the metal may be achieved by exposing the film to UV
rays in an ozone atmosphere (O.sub.3). Other oxidative agents or
atmospheres can be utilized for this purpose, e.g. exposing the
substrate film to oxygen (O.sub.2) during metal deposition. In
accordance with another embodiment, the electrode material 30 may
include a material selected from the group including silver oxide,
lithium manganese oxide (LiMn.sub.2O.sub.4), lithium iron phosphate
(LiFePO.sub.4), LiNi.sub.xCo.sub.yAl.sub.zO.sub.2,
LiNi.sub.xCo.sub.yMn.sub.zO.sub.2, and a combination thereof.
Any suitable metal deposition technique may be employed. PVD may
offer faster deposition of thick (greater than 10 .mu.m) metallic
layers than other processes. Electroplating may be alternatively
used, if the required thickness of the active material exceeds the
thickness possible via PVD or sputtering, for the film. The
thickness of the current collector is generally less than the
thickness of the active material and may be formed by any suitable
technique. Chemical fluid deposition offers the advantage of being
a lower temperature process and may reduce the number of processing
steps. While sintering may be used to deposit silver powder onto
the substrate, this process may be less desirable because of the
required processing temperatures. The surface finish of the final
electrode structure depends strongly on the temperature of the
substrate and on the evaporation technique used. PVD is conducted
at lower substrate temperatures, creating substrates of higher
porosity and rougher surface finishes. The deposited films may be
amorphous, and may require subsequent heating to induce
re-crystallization. The porous structure is beneficial for battery
electrodes employing liquid electrolytes because of the active
surface area afforded, and the permeability to electrolyte, while
maintaining electronic conductivity and mechanical integrity.
If necessary, multiple substrates may be prepared on a wafer or
other base structure. After etching, metal deposition and
oxidization steps are completed as needed to achieve proper
specific and gravimetric energy and power characteristics.
Individual substrates may be separated from the wafer using
standard cutting techniques. Cooling water should not be used
during dicing of anode parts to prevent oxidation of the zinc.
Sub-millimeter diameter channels or apertures 28, for example, on
the order of 100 .mu.m diameter, are formed in the substrate 32 to
allow for the introduction of electrolyte, for example, potassium
hydroxide (KOH), diethyl carbonate (DEC), dimethyl carbonate (DMC),
ethylene carbonate (EC), ethyl methyl carbonate (EMC), propylene
carbonate (PC), or other electrolyte which conducts ions but is
electrically neutral, into a completed microarchitectured battery
structure 12 with simultaneous evacuation of air. Alternatively,
geltype electrolytes may be used and enclosed within the
microbattery structure during the joining and sealing of the
sections, or may be inserted afterward, using passages formed in
the substrate suitable for this purpose.
Micromachine drilling or chemical drilling may be used to form the
apertures 28. Optional glass channels (not depicted) may be
inserted into the formed holes and secured therein using a fast
curing epoxy resin. Following introduction of the electrolyte, the
glass channels, if present, may be cut from the package and the
apertures 28 sealed using epoxy.
In the foregoing example, individual substrates are separated prior
to assembly into battery structures. Plural batteries may be
assembled prior to separation. After completion of the metal
deposition steps, an adhesive, for example one or more dry adhesive
sheets or screen printed wet adhesive, may be disposed on one or
both of the wafers. The wafers may then be brought together in a
wafer-adhesive-separator-adhesive-wafer sandwich, the adhesive
cured and then individual batteries separated.
Plural processing of the micromachined battery further permits
manufacture of multiple cell micromachined batteries. During the
separation process, multiple cells may be left joined (see battery
cells 12' depicted in FIG. 3). During formation of the current
collectors 34 and the conductive taps 36, the conductive taps may
be formed to link the multiple cells (see conductive taps 36') to
provide a single output of the multiple cell micromachined
battery.
The actual electrode, electrolyte and separator materials may be
chosen for the application and may be improved using known
optimization techniques. One such optimization technique is
described by Albano, et al., Design of an Implantable Power Supply
for an Intraocular Sensor, Using POWER (Power Optimization for
Wireless Energy Requirements) and by Cook, et al., POWER (power
optimization for wireless energy requirements): A MATLAB based
algorithm for design of hybrid energy systems, Journal of Power
Sources 159 (2006) 758-780.
Nickel cell chemistries offer the advantage of being radio
frequency rechargeable. Silver cell chemistries may enhance
reliability and provide discharge current stability. Thin film
technologies, including lithium chemistries, pose potential
processing difficulties when combining with a MEMS device due to
potentially high processing temperatures required in the MEMS
processing. However, some cell chemistries may are capable of
withstanding temperatures up to 200.degree. C.
The polymer bond to silicon, joining the micromachined battery 12
to the MEMS device 10 may be enhanced by first coating both parts
with evaporated gold. A plasma enhanced chemical vapor deposition
(PECVD) silicon nitride film may also enhance bonding. Gold and
silicon are known to create a eutectic compound that has a much
lower melting point than the pure metals. A liquid film is created
in the joining process that bonds the two parts upon cooling and
solidification.
Embodiments of batteries in accordance with the present invention
may have one or more of the following characteristics:
1) formed and integrated at the same time of manufacturing with a
MEMS device;
2) small and lightweight enabling creation of autonomous and remote
sensor networks;
3) present high gravimetric and volumetric energy and power and
Faradic efficiency superior to commercial batteries with the
potential to meet (.about.27 mWh/cm.sup.2);
4) low internal resistance and low power leakage due to high
precision manufacturing;
5) thin film deposited electrodes;
6) stackable and/or layered electrodes to achieve higher
voltages;
7) suitable for configuration as thin-film flat cells, prismatic
stacks of cells, cylindrical cells or spirally wound cell
8) amendable to primary or secondary electrochemistries
9) compatible with solid thin-film electrolyte or liquid or gel
solutions of electrolyte
10) capable of hermetic sealing;
11) mass produceable potentially reducing cost;
12) scalable to macroscopic battery size.
While application of batteries in accordance with the herein
described embodiments in MEMS devices is apparent, the techniques
are fully scalable, and large-scale deposited batteries are
possible and desirable. Demonstration of the inventive technology
for a small battery illustrates and validates the approach. The
invention and embodiments of the invention therefore provide:
A) design and fabrication of optimized power supplies for MEMS with
significantly reduced size and improved energy and power properties
that allow integration at the time of manufacture or after
manufacturing of the device is complete;
B) a fabrication technique based on thin-film deposition, allowing
small scale, low-cost, and integrateable fabrication for CMOS
systems;
C) characterization of capacity and lifetime of microbattery
stacks, arrangements and multi-cells configurations; and
D) a process for forming microscopic electrode films on rigid or
flexible substrates and a liquid, gel or solid electrolyte spacing
by application of microarchitecturing techniques to the
substrates.
While the invention is described in terms of several preferred
embodiments of mounting assemblies that may be used in connection
with fault protection devices, it will be appreciated that the
invention is not limited to such devices. The inventive concepts
may be employed in connection with any number of devices and
structures. Moreover, while features of various embodiments are
shown and described in combination, the features may be implemented
individually each such single implementation being within the scope
of the invention.
While the present disclosure is susceptible to various
modifications and alternative forms, certain embodiments are shown
by way of example in the drawings and the herein described
embodiments. It will be understood, however, that this disclosure
is not intended to limit the invention to the particular forms
described, but to the contrary, the invention is intended to cover
all modifications, alternatives, and equivalents defined by the
appended claims.
It should also be understood that, unless a term is expressly
defined in this patent using the sentence "As used herein, the term
`.sub.------------` is hereby defined to mean . . . " or a similar
sentence, there is no intent to limit the meaning of that term,
either expressly or by implication, beyond its plain or ordinary
meaning, and such term should not be interpreted to be limited in
scope based on any statement made in any section of this patent
(other than the language of the claims). To the extent that any
term recited in the claims at the end of this patent is referred to
in this patent in a manner consistent with a single meaning, that
is done for sake of clarity only so as to not confuse the reader,
and it is not intended that such claim term by limited, by
implication or otherwise, to that single meaning. Unless a claim
element is defined by reciting the word "means" and a function
without the recital of any structure, it is not intended that the
scope of any claim element be interpreted based on the application
of 35 U.S.C. .sctn.112, sixth paragraph.
* * * * *